Canonical Allele Identifier: CA771295227
Gene: SPRED2 HGNC NCBI

Linked Data

dbSNP Id: rs1454312256
MyVariant Identifiers: chr2:g.65608591del (hg19) chr2:g.65381457del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381457del , CM000664.2:g.65381457del GRCh38
NC_000002.11:g.65608591del , CM000664.1:g.65608591del GRCh37
NC_000002.10:g.65462095del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356388.9:c.27-36561del MANE Select ENSP00000348753.4:n.27-36561del
ENST00000356388.8:c.27-36561del ENSP00000348753.4:n.27-36561del
ENST00000440972.1:c.27-36561del ENSP00000406481.1:n.27-36561del
NM_181784.2:c.27-36561del NP_861449.2:n.27-36561del
XM_005264200.3:c.27-36561del XP_005264257.2:n.27-36561del
XM_005264202.3:c.27-36561del XP_005264259.1:n.27-36561del
XM_006711966.1:c.27-36561del XP_006712029.1:n.27-36561del
XM_005264200.5:c.27-36561del XP_005264257.2:n.27-36561del
XM_005264202.5:c.27-36561del XP_005264259.1:n.27-36561del
NM_181784.3:c.27-36561del MANE Select NP_861449.2:n.27-36561del
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